Canonical Allele Identifier: CA891838196

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965452_87965453delinsTA , CM000672.2:g.87965452_87965453delinsTA	GRCh38
NC_000010.10:g.89725209_89725210delinsTA , CM000672.1:g.89725209_89725210delinsTA	GRCh37
NC_000010.9:g.89715189_89715190delinsTA	NCBI36
NG_007466.2:g.107014_107015delinsTA , LRG_311:g.107014_107015delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1285_1286delinsTA	ENSP00000514759.2:p.Thr429Ter
ENST00000710265.1:c.*221_*222delinsTA	ENSP00000518161.1:n.*221_*222delinsTA
ENST00000688158.2:n.1927_1928delinsTA
ENST00000688922.2:c.*1022_*1023delinsTA	ENSP00000508742.2:n.*1022_*1023delinsTA
ENST00000700021.1:c.1147_1148delinsTA	ENSP00000514757.1:p.Thr383Ter
ENST00000700022.1:c.*531_*532delinsTA	ENSP00000514758.1:n.*531_*532delinsTA
ENST00000700023.1:n.2350_2351delinsTA
ENST00000700024.1:n.2584_2585delinsTA
ENST00000706954.1:c.1192_1193delinsTA	ENSP00000516674.1:p.Thr398Ter
ENST00000706955.1:c.*1227_*1228delinsTA	ENSP00000516675.1:n.*1227_*1228delinsTA
ENST00000686459.1:c.*778_*779delinsTA	ENSP00000508909.1:n.*778_*779delinsTA
ENST00000688158.1:c.*1303_*1304delinsTA	ENSP00000509254.1:n.*1303_*1304delinsTA
ENST00000688308.1:c.1192_1193delinsTA	ENSP00000508752.1:p.Thr398Ter
ENST00000688922.1:c.1113_1114delinsTA
ENST00000693560.1:c.1711_1712delinsTA	ENSP00000509861.1:p.Thr571Ter
ENST00000371953.8:c.1192_1193delinsTA MANE Select	ENSP00000361021.3:p.Thr398Ter
ENST00000371953.7:c.1192_1193delinsTA	ENSP00000361021.3:p.Thr398Ter
NM_000314.5:c.1192_1193delinsTA	NP_000305.3:p.Thr398Ter
NM_000314.6:c.1192_1193delinsTA	NP_000305.3:p.Thr398Ter
NM_001304717.2:c.1711_1712delinsTA	NP_001291646.2:p.Thr571Ter
NM_001304718.1:c.601_602delinsTA	NP_001291647.1:p.Thr201Ter
XM_006717926.2:c.1147_1148delinsTA	XP_006717989.1:p.Thr383Ter
XM_011539982.1:c.1096_1097delinsTA	XP_011538284.1:p.Thr366Ter
XR_945791.1:n.1762_1763delinsTA
NM_000314.7:c.1192_1193delinsTA	NP_000305.3:p.Thr398Ter
NM_001304717.5:c.1711_1712delinsTA	NP_001291646.4:p.Thr571Ter
NM_001304718.2:c.601_602delinsTA	NP_001291647.1:p.Thr201Ter
NM_000314.8:c.1192_1193delinsTA MANE Select	NP_000305.3:p.Thr398Ter